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rs587781924

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781924(-;-)
Make rs587781924(-;T)
Make rs587781924(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803559
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781924
ebirs587781924
HLIrs587781924
Exacrs587781924
Varsomers587781924
Maprs587781924
PheGenIrs587781924
hapmaprs587781924
1000 genomesrs587781924
hgdprs587781924
ensemblrs587781924
gopubmedrs587781924
geneviewrs587781924
scholarrs587781924
googlers587781924
pharmgkbrs587781924
gwascentralrs587781924
openSNPrs587781924
23andMers587781924
23andMe allrs587781924
SNP Nexus

SNPshotrs587781924
SNPdbers587781924
MSV3drs587781924
GWAS Ctlgrs587781924
Max Magnitude0
ClinVar
Risk rs587781924(T;T)
Alt rs587781924(T;T)
Reference rs587781924(;)
Significance Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030698dupT
CLNSRC
CLNACC RCV000121582.1, RCV000130275.2,